Department of Microbiology and Immunology, Temple University Lewis Katz School of Medicine, Philadelphia, PA 19140, USA. Email:
Sci Signal. 2017 Aug 15;10(492):eaan3589. doi: 10.1126/scisignal.aan3589.
Pathogens deploy immune evasion strategies to successfully establish infections within their hosts. Naturally, the host responds by acquiring mechanisms to counter these strategies. There is increasing evidence that the three interleukin-36 (IL-36) cytokines, IL-36α, IL-36β and IL-36γ, play important roles in host immunity. With a focus on the skin as a target for microbial and viral invasion, the current knowledge of IL-36 functions is reviewed. Furthermore, the hypothesis that the IL-36s have evolved to counteract virulence factors is presented using viruses as an example. The IL-36s are related to IL-1α, IL-1β, IL-18, and IL-33. Numerous viruses affecting the skin have developed immune evasion strategies that neutralize IL-1α, IL-1β, or IL-18 signaling or combinations of these pathways. Through small differences in activation mechanisms and receptor utilization, it is possible that IL-36 signaling may proceed unhindered in the presence of these viral inhibitors. Thus, one physiological function of the IL-36s may be to counteract microbial immune evasion.
病原体利用免疫逃避策略在宿主体内成功建立感染。自然,宿主通过获得机制来对抗这些策略做出反应。越来越多的证据表明,三种白细胞介素-36(IL-36)细胞因子,IL-36α、IL-36β和 IL-36γ,在宿主免疫中发挥重要作用。本文重点关注皮肤作为微生物和病毒入侵的靶标,综述了 IL-36 功能的现有知识。此外,本文还提出了一个假设,即 IL-36 是为了对抗病毒的毒力因子而进化而来的,以病毒为例进行了说明。IL-36 与 IL-1α、IL-1β、IL-18 和 IL-33 有关。许多影响皮肤的病毒已经开发出免疫逃避策略,以中和 IL-1α、IL-1β 或 IL-18 信号通路或这些途径的组合。通过激活机制和受体利用的微小差异,IL-36 信号通路在存在这些病毒抑制剂的情况下可能不受阻碍地进行。因此,IL-36 的一个生理功能可能是对抗微生物的免疫逃避。